5'-O-(4,4'-Dimethoxy-4''-(1H,1H,2H,2H-perfluorodecyl)trityl)thymidine 3'-CE phosphoramidite

≥95%

Reagent Code: #221353
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CAS Number 902456-09-1

science Other reagents with same CAS 902456-09-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1206.92 g/mol
Formula C₅₀H₅₂F₁₇N₄O₉P
badge Registry Numbers
MDL Number MFCD08062090
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in solid-phase oligonucleotide synthesis, this compound enables the incorporation of thymidine residues into DNA strands with high efficiency and specificity. Its primary application lies in the preparation of DNA sequences for research and diagnostic purposes, particularly in antisense technology, gene expression studies, and probe development. The fluorinated trityl protecting group improves compatibility with organic solvents and reduces the formation of byproducts during synthesis, facilitating more efficient automated production. Additionally, the dimethoxytrityl moiety allows for easy monitoring of coupling efficiency through the release of the colored trityl cation. The phosphoramidite group ensures compatibility with automated DNA synthesizers, supporting rapid and scalable production of custom nucleic acid sequences.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,980.00

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5'-O-(4,4'-Dimethoxy-4''-(1H,1H,2H,2H-perfluorodecyl)trityl)thymidine 3'-CE phosphoramidite
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Used in solid-phase oligonucleotide synthesis, this compound enables the incorporation of thymidine residues into DNA strands with high efficiency and specificity. Its primary application lies in the preparation of DNA sequences for research and diagnostic purposes, particularly in antisense technology, gene expression studies, and probe development. The fluorinated trityl protecting group improves compatibility with organic solvents and reduces the formation of byproducts during synthesis, facilitating

Used in solid-phase oligonucleotide synthesis, this compound enables the incorporation of thymidine residues into DNA strands with high efficiency and specificity. Its primary application lies in the preparation of DNA sequences for research and diagnostic purposes, particularly in antisense technology, gene expression studies, and probe development. The fluorinated trityl protecting group improves compatibility with organic solvents and reduces the formation of byproducts during synthesis, facilitating more efficient automated production. Additionally, the dimethoxytrityl moiety allows for easy monitoring of coupling efficiency through the release of the colored trityl cation. The phosphoramidite group ensures compatibility with automated DNA synthesizers, supporting rapid and scalable production of custom nucleic acid sequences.

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